ClinVar Miner

List of variants in gene TTN reported by New York Genome Center

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 96
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.35409T>G (p.Ile11803Met) rs186992412 0.00129
NM_001267550.2(TTN):c.32186C>T (p.Thr10729Met) rs115119858 0.00125
NM_001267550.2(TTN):c.57370G>A (p.Val19124Ile) rs142841000 0.00051
NM_001267550.2(TTN):c.7523A>G (p.His2508Arg) rs146970027 0.00041
NM_001267550.2(TTN):c.36196G>A (p.Asp12066Asn) rs140655598 0.00039
NM_001267550.2(TTN):c.89314G>A (p.Glu29772Lys) rs200503016 0.00019
NM_001267550.2(TTN):c.50212G>A (p.Glu16738Lys) rs148018042 0.00017
NM_001267550.2(TTN):c.92696T>C (p.Ile30899Thr) rs373727636 0.00016
NM_001267550.2(TTN):c.14869A>C (p.Thr4957Pro) rs780405420 0.00015
NM_001267550.2(TTN):c.75490G>A (p.Asp25164Asn) rs192468365 0.00014
NM_001267550.2(TTN):c.57242T>C (p.Ile19081Thr) rs78509062 0.00012
NM_001267550.2(TTN):c.76673A>T (p.Asp25558Val) rs201095164 0.00011
NM_001267550.2(TTN):c.266C>G (p.Ala89Gly) rs200165636 0.00010
NM_001267550.2(TTN):c.5314A>G (p.Ser1772Gly) rs150725992 0.00009
NM_001267550.2(TTN):c.33340+5A>C rs373367032 0.00007
NM_001267550.2(TTN):c.11667G>T (p.Glu3889Asp) rs377423256 0.00006
NM_001267550.2(TTN):c.54518C>A (p.Pro18173Gln) rs794729458 0.00006
NM_001267550.2(TTN):c.55435G>A (p.Val18479Ile) rs559712998 0.00006
NM_001267550.2(TTN):c.83978C>A (p.Thr27993Asn) rs377614000 0.00006
NM_001267550.2(TTN):c.15148G>T (p.Gly5050Trp) rs908686601 0.00005
NM_001267550.2(TTN):c.71699G>A (p.Arg23900Gln) rs369292052 0.00005
NM_001267550.2(TTN):c.89711G>A (p.Arg29904His) rs397517744 0.00005
NM_001267550.2(TTN):c.76661C>G (p.Ala25554Gly) rs879087699 0.00004
NM_001267550.2(TTN):c.94507G>A (p.Ala31503Thr) rs375657115 0.00004
NM_001267550.2(TTN):c.99310C>T (p.Arg33104Cys) rs766169253 0.00004
NM_001267550.2(TTN):c.101479C>T (p.Arg33827Cys) rs372067498 0.00003
NM_001267550.2(TTN):c.40723+1G>T rs371770198 0.00003
NM_001267550.2(TTN):c.65410T>C (p.Trp21804Arg) rs745626132 0.00003
NM_001267550.2(TTN):c.78323A>G (p.Gln26108Arg) rs370963021 0.00003
NM_001267550.2(TTN):c.102761T>C (p.Leu34254Pro) rs556155561 0.00002
NM_001267550.2(TTN):c.35470+4T>C rs1389073196 0.00002
NM_001267550.2(TTN):c.102274C>T (p.Arg34092Cys) rs765435004 0.00001
NM_001267550.2(TTN):c.11282T>C (p.Ile3761Thr) rs758073208 0.00001
NM_001267550.2(TTN):c.12026A>G (p.Tyr4009Cys) rs753367343 0.00001
NM_001267550.2(TTN):c.13205C>T (p.Ala4402Val) rs756976503 0.00001
NM_001267550.2(TTN):c.37433C>T (p.Pro12478Leu) rs1302865780 0.00001
NM_001267550.2(TTN):c.41423G>A (p.Arg13808His) rs764850788 0.00001
NM_001267550.2(TTN):c.42714T>A (p.His14238Gln) rs1438979717 0.00001
NM_001267550.2(TTN):c.54418C>T (p.Arg18140Ter) rs747236787 0.00001
NM_001267550.2(TTN):c.55660C>T (p.Arg18554Ter) rs1483931960 0.00001
NM_001267550.2(TTN):c.60524C>T (p.Pro20175Leu) rs771358314 0.00001
NM_001267550.2(TTN):c.67348+1G>A rs758279518 0.00001
NM_001267550.2(TTN):c.69420del (p.Gly23141fs) rs1330960948 0.00001
NM_001267550.2(TTN):c.725A>G (p.Asp242Gly) rs773021696 0.00001
NM_001267550.2(TTN):c.72713C>T (p.Ser24238Leu) rs786205303 0.00001
NM_001267550.2(TTN):c.94855C>T (p.Arg31619Ter) rs869312121 0.00001
NM_001267550.2(TTN):c.95665G>A (p.Ala31889Thr) rs1025105445 0.00001
NM_001267550.2(TTN):c.98917A>G (p.Ile32973Val) rs773080115 0.00001
NM_001267550.2(TTN):c.100397G>A (p.Arg33466His) rs189626540
NM_001267550.2(TTN):c.102455A>G (p.His34152Arg)
NM_001267550.2(TTN):c.106572G>T (p.Lys35524Asn)
NM_001267550.2(TTN):c.12151G>T (p.Asp4051Tyr)
NM_001267550.2(TTN):c.1863A>C (p.Lys621Asn)
NM_001267550.2(TTN):c.19655C>T (p.Thr6552Ile)
NM_001267550.2(TTN):c.22496C>T (p.Thr7499Ile)
NM_001267550.2(TTN):c.23329A>G (p.Thr7777Ala)
NM_001267550.2(TTN):c.26333G>C (p.Arg8778Thr)
NM_001267550.2(TTN):c.26653T>G (p.Ser8885Ala)
NM_001267550.2(TTN):c.29285C>T (p.Thr9762Ile)
NM_001267550.2(TTN):c.33277G>A (p.Glu11093Lys)
NM_001267550.2(TTN):c.3476G>T (p.Arg1159Leu) rs149883066
NM_001267550.2(TTN):c.35224A>G (p.Lys11742Glu)
NM_001267550.2(TTN):c.35363A>G (p.Glu11788Gly)
NM_001267550.2(TTN):c.36267_36280+16del rs745871962
NM_001267550.2(TTN):c.38488G>A (p.Ala12830Thr)
NM_001267550.2(TTN):c.38918C>G (p.Pro12973Arg)
NM_001267550.2(TTN):c.40761_40766del (p.Glu13588_Pro13589del)
NM_001267550.2(TTN):c.41002CCT[1] (p.Pro13669del) rs747793660
NM_001267550.2(TTN):c.42439C>T (p.Pro14147Ser) rs1559970037
NM_001267550.2(TTN):c.43156G>A (p.Gly14386Arg)
NM_001267550.2(TTN):c.44053G>A (p.Glu14685Lys)
NM_001267550.2(TTN):c.50869A>G (p.Ile16957Val) rs372013419
NM_001267550.2(TTN):c.52405+4A>G
NM_001267550.2(TTN):c.53741A>C (p.Lys17914Thr)
NM_001267550.2(TTN):c.628A>G (p.Thr210Ala)
NM_001267550.2(TTN):c.64880G>T (p.Gly21627Val) rs2154180072
NM_001267550.2(TTN):c.64906G>C (p.Ala21636Pro)
NM_001267550.2(TTN):c.65143C>G (p.Arg21715Gly) rs766522121
NM_001267550.2(TTN):c.66753T>G (p.Tyr22251Ter) rs2047743679
NM_001267550.2(TTN):c.71266G>A (p.Gly23756Ser)
NM_001267550.2(TTN):c.71602C>T (p.Arg23868Ter) rs397517689
NM_001267550.2(TTN):c.72988C>T (p.Pro24330Ser)
NM_001267550.2(TTN):c.74597C>G (p.Thr24866Arg)
NM_001267550.2(TTN):c.74609C>T (p.Ala24870Val)
NM_001267550.2(TTN):c.80294T>C (p.Val26765Ala)
NM_001267550.2(TTN):c.81905A>G (p.Lys27302Arg) rs2154162241
NM_001267550.2(TTN):c.82682T>C (p.Phe27561Ser)
NM_001267550.2(TTN):c.85969A>T (p.Lys28657Ter) rs72648224
NM_001267550.2(TTN):c.86729AAG[1] (p.Glu28911del) rs727504797
NM_001267550.2(TTN):c.88379T>C (p.Leu29460Pro)
NM_001267550.2(TTN):c.89047G>A (p.Val29683Ile)
NM_001267550.2(TTN):c.89136C>A (p.Asn29712Lys)
NM_001267550.2(TTN):c.89993C>A (p.Ser29998Ter) rs376543931
NM_001267550.2(TTN):c.91583T>G (p.Phe30528Cys)
NM_001267550.2(TTN):c.94520T>C (p.Val31507Ala)
NM_001267550.2(TTN):c.98810_98811del (p.Lys32937fs)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.